JP2005508337A5 - - Google Patents

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Publication number
JP2005508337A5
JP2005508337A5 JP2003530699A JP2003530699A JP2005508337A5 JP 2005508337 A5 JP2005508337 A5 JP 2005508337A5 JP 2003530699 A JP2003530699 A JP 2003530699A JP 2003530699 A JP2003530699 A JP 2003530699A JP 2005508337 A5 JP2005508337 A5 JP 2005508337A5
Authority
JP
Japan
Prior art keywords
hydrogen
alkyl
compound
halogen
physiologically functional
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2003530699A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005508337A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2002/030150 external-priority patent/WO2003027111A1/en
Publication of JP2005508337A publication Critical patent/JP2005508337A/ja
Publication of JP2005508337A5 publication Critical patent/JP2005508337A5/ja
Pending legal-status Critical Current

Links

JP2003530699A 2001-09-27 2002-09-24 化合物 Pending JP2005508337A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32601201P 2001-09-27 2001-09-27
PCT/US2002/030150 WO2003027111A1 (en) 2001-09-27 2002-09-24 Chemical compounds

Publications (2)

Publication Number Publication Date
JP2005508337A JP2005508337A (ja) 2005-03-31
JP2005508337A5 true JP2005508337A5 (de) 2005-12-22

Family

ID=23270442

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003530699A Pending JP2005508337A (ja) 2001-09-27 2002-09-24 化合物

Country Status (7)

Country Link
US (2) US7015231B2 (de)
EP (1) EP1430053B1 (de)
JP (1) JP2005508337A (de)
AT (1) ATE343575T1 (de)
DE (1) DE60215682T2 (de)
ES (1) ES2275021T3 (de)
WO (1) WO2003027111A1 (de)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002020513A1 (en) 2000-09-01 2002-03-14 Glaxo Group Limited Oxindole derivatives
WO2002020479A1 (en) 2000-09-01 2002-03-14 Glaxo Group Limited Substituted oxindole derivatives as tyrosine kinase inhibitors
JP2005508337A (ja) * 2001-09-27 2005-03-31 スミスクライン ビーチャム コーポレーション 化合物
PT2383268E (pt) 2005-02-04 2015-12-21 Astrazeneca Ab Derivados de pirazolilaminopiridina úteis como inibidores de quinase
MX2007009842A (es) * 2005-02-16 2007-08-23 Astrazeneca Ab Compuestos quimicos.
PT1853588E (pt) 2005-02-16 2008-08-25 Astrazeneca Ab Compostos químicos
EP1945631B8 (de) 2005-10-28 2013-01-02 AstraZeneca AB 4-(3-aminopyrazol)pyrimidinderivate zur verwendung als tyrosinkinaseinhibitoren bei der behandlung von krebs
US7514435B2 (en) 2005-11-18 2009-04-07 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
KR20090004976A (ko) 2006-04-19 2009-01-12 아스테라스 세이야쿠 가부시키가이샤 아졸카르복사미드 유도체
WO2009054468A1 (ja) 2007-10-24 2009-04-30 Astellas Pharma Inc. アゾールカルボキサミド化合物又はその塩
CA2711865A1 (en) 2008-01-11 2009-07-16 Astellas Pharma Inc. A pathological animal model simultaneously developing testicular pain or discomfort behaviors and urinary frequency
BRPI0922224A2 (pt) 2008-12-08 2016-08-02 Vm Pharma Llc composições de inibidores de proteína tirosina quiinase receptora.
JP5778755B2 (ja) * 2010-04-15 2015-09-16 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung ヒドロキノンの製造方法
US8999992B2 (en) 2013-03-15 2015-04-07 Vm Pharma Llc Crystalline forms of tryosine kinase inhibitors and their salts
CN103804273B (zh) * 2014-01-27 2016-06-15 贵州大学 氧化吲哚与茚三酮双季碳拼接衍生物及其制备方法
TWI672141B (zh) 2014-02-20 2019-09-21 美商醫科泰生技 投予ros1突變癌細胞之分子
US10301271B2 (en) 2014-09-17 2019-05-28 Purdue Pharma L.P. Crystalline forms of tyrosine kinase inhibitors and their salts
AU2015355220B2 (en) 2014-12-02 2020-02-27 Ignyta, Inc. Combinations for the treatment of neuroblastoma
WO2017106492A1 (en) 2015-12-18 2017-06-22 Ignyta, Inc. Combinations for the treatment of cancer
AU2018302170B2 (en) 2017-07-19 2024-02-29 Ignyta, Inc. Pharmaceutical compositions comprising entrectinib
EP3697390A1 (de) 2017-10-17 2020-08-26 Ignyta, Inc. Pharmazeutische zusammensetzungen und darreichungsformen
EA202192575A1 (ru) 2019-03-21 2022-01-14 Онксео Соединения dbait в сочетании с ингибиторами киназ для лечения рака
US20220401436A1 (en) 2019-11-08 2022-12-22 INSERM (Institute National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9423997D0 (en) * 1994-11-28 1995-01-11 Erba Carlo Spa Substituted 3-arylidene-7-azaoxindole compounds and process for their preparation
GB9716557D0 (en) * 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
GB9721437D0 (en) * 1997-10-10 1997-12-10 Glaxo Group Ltd Heteroaromatic compounds and their use in medicine
CA2383623A1 (en) 1998-08-04 2000-02-17 Sugen, Inc. 3-methylidenyl-2-indolinone modulators of protein kinase
JP2005508337A (ja) * 2001-09-27 2005-03-31 スミスクライン ビーチャム コーポレーション 化合物

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